DK151803C - METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF - Google Patents

METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF

Info

Publication number
DK151803C
DK151803C DK400679A DK400679A DK151803C DK 151803 C DK151803 C DK 151803C DK 400679 A DK400679 A DK 400679A DK 400679 A DK400679 A DK 400679A DK 151803 C DK151803 C DK 151803C
Authority
DK
Denmark
Prior art keywords
formula
lower alkyl
hydrogen
acceptable salts
pyrrol
Prior art date
Application number
DK400679A
Other languages
Danish (da)
Other versions
DK400679A (en
DK151803B (en
Inventor
Elvio Bellasio
Nunzio Di Mola
Ambrogio Campi
Emiliana Baldoli
Original Assignee
Lepetit Spa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lepetit Spa filed Critical Lepetit Spa
Publication of DK400679A publication Critical patent/DK400679A/en
Publication of DK151803B publication Critical patent/DK151803B/en
Application granted granted Critical
Publication of DK151803C publication Critical patent/DK151803C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/26Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
    • C07D237/30Phthalazines
    • C07D237/34Phthalazines with nitrogen atoms directly attached to carbon atoms of the nitrogen-containing ring, e.g. hydrazine radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/20Nitrogen atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pyrrole Compounds (AREA)

Abstract

New N-pyrrolyl-3-pyridazine-amines having a further aminic substituent in the 6 position of the formula (I), <CHEM> wherein R, R1, R2 and R3 are hydrogen or lower alkyl, R4 is e.g. hydrogen or lower alkyl, R5 and R6 are e.g. lower alkyl or taken together with the adjacent nitrogen atom represent a saturated 5 - 6 membered heterocyclic ring which may contain a further heteroatom, R7 and R8 represent hydrogen or, taken together, a 1,3-butadienylene radical forming a benzo system fused with the pyridazine ring, for example N-2,5-dimethyl-1H-pyrrol-1-yl)- 6-morpholino-3-pyridazineamine or N-(2,5-dimethyl-1H-pyrrol- 1-yl)-4-(4-hydroxypiperidino)-1-phthalazineamine, and their pharmaceutically acceptable salts are made e.g. by contacting a hydrazino derivate of the formula (II), wherein the substituents have the same meaning as above or an acid addition salt thereof with a dicarbonyl compound of the formula (III), wherein the substituents have the same meaning as above, or a functional derivative thereof in the presence of an acid catalyst at a temperature between 15 DEG C and 120 DEG C. The new compounds can be used as antihypertensive agents.
DK400679A 1978-10-02 1979-09-25 METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF DK151803C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB7838898 1978-10-02
GB7838898 1978-10-02

Publications (3)

Publication Number Publication Date
DK400679A DK400679A (en) 1980-04-03
DK151803B DK151803B (en) 1988-01-04
DK151803C true DK151803C (en) 1988-06-13

Family

ID=10500040

Family Applications (1)

Application Number Title Priority Date Filing Date
DK400679A DK151803C (en) 1978-10-02 1979-09-25 METHOD OF ANALOGUE FOR THE PREPARATION OF N-PYRROLYLPYRIDAZINAMINE DERIVATIVES OR PHARMACEUTICAL ACCEPTABLE SALTS THEREOF

Country Status (15)

Country Link
EP (1) EP0009655B1 (en)
JP (1) JPS5569577A (en)
AT (1) ATE3294T1 (en)
AU (1) AU529482B2 (en)
CA (1) CA1144165A (en)
DE (1) DE2965377D1 (en)
DK (1) DK151803C (en)
ES (1) ES484616A1 (en)
FI (1) FI65998C (en)
GR (1) GR69856B (en)
IE (1) IE49017B1 (en)
IL (1) IL58256A (en)
NO (1) NO151620C (en)
YU (1) YU41886B (en)
ZA (1) ZA794923B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1150070B (en) * 1980-12-22 1986-12-10 Lepetit Spa PROCEDURE FOR PREPARING N-PYROLIPYRIDAZINAMINIC DERIVATIVES
US5254622A (en) * 1988-12-09 1993-10-19 Asahi Kasei Kogyo Kabushiki Kaisha ABS resin compositions and molded articles thereof having improved coating performances
RU2006105716A (en) * 2003-07-30 2007-09-10 Зинон Фармасьютиклз Инк. (Ca) Pyridazine derivatives and their use as therapeutic agents
CA2580857A1 (en) 2004-09-20 2006-09-28 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
EP1799668A1 (en) 2004-09-20 2007-06-27 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as mediators of stearoyl-coa desaturase
TW200626138A (en) 2004-09-20 2006-08-01 Xenon Pharmaceuticals Inc Heterocyclic derivatives and their use as therapeutic agents
CA2580787A1 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-coa desaturase enzymes
CA2580845A1 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase
BRPI0515505A (en) 2004-09-20 2008-07-29 Xenon Pharmaceuticals Inc heterocyclic derivatives and their use as stearoyl coat desaturase inhibitors
EP1799664A1 (en) 2004-09-20 2007-06-27 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
US8541457B2 (en) 2005-06-03 2013-09-24 Xenon Pharmaceuticals Inc. Aminothiazole derivatives as human stearoyl-CoA desaturase inhibitors
USD916552S1 (en) * 2019-07-26 2021-04-20 Spectrum Diversified Designs, Llc Trivet
JP7181481B2 (en) * 2021-02-08 2022-12-01 株式会社カプコン Information processing system, program and information processing method

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1168334A (en) * 1967-01-25 1969-10-22 Lepetit Spa New Pharmacologically Active Pyridazines
GB1378102A (en) * 1972-03-14 1974-12-18 Lepetit Spa Antihypertensive compositions
GB1408362A (en) * 1973-05-25 1975-10-01 Lepetit Spa 2-pyrrol-1-yl amino 4,5-dihydro-1-h-imidazole derivatives
AU477837B2 (en) * 1973-05-30 1974-12-05 I. S. F. Sp. A New anti-hypertensive compounds having a high therapeutic index and a long-term hypotensive effect
ES431009A1 (en) * 1974-05-09 1976-10-16 Isf Spa Process for the preparation of benzylidene derivatives

Also Published As

Publication number Publication date
IE791866L (en) 1980-04-02
FI792832A (en) 1980-04-03
GR69856B (en) 1982-07-19
IE49017B1 (en) 1985-07-10
JPS5569577A (en) 1980-05-26
DE2965377D1 (en) 1983-06-16
AU529482B2 (en) 1983-06-09
FI65998B (en) 1984-04-30
EP0009655A1 (en) 1980-04-16
ES484616A1 (en) 1980-05-16
YU41886B (en) 1988-02-29
NO793151L (en) 1980-04-08
NO151620B (en) 1985-01-28
ZA794923B (en) 1980-09-24
YU237479A (en) 1983-02-28
IL58256A (en) 1984-02-29
AU5086679A (en) 1980-04-17
FI65998C (en) 1984-08-10
EP0009655B1 (en) 1983-05-11
IL58256A0 (en) 1979-12-30
NO151620C (en) 1985-05-08
ATE3294T1 (en) 1983-05-15
CA1144165A (en) 1983-04-05
DK400679A (en) 1980-04-03
JPH0321553B2 (en) 1991-03-22
DK151803B (en) 1988-01-04

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Legal Events

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PBP Patent lapsed